FDA Device recall Z-2417-2024
Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas t…
- FDA Device
- Class II
- ongoing
- Published 2024-07-31
On 2024-07-31 the FDA classified a Class II recall of Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas t… by Securitas Healthcare, citing there is a risk that alarms will not be received by the Arial Wireless Emergency Call System and premature depletion of the battery.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2417-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-06-20 |
| Published | 2024-07-31 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Securitas Healthcare |
| Distribution | CA, MD, MN, MS, NE, OR, TX, WA, WI |
Product
Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas to allow immediate staff response.
Reason
There is a risk that alarms will not be received by the Arial Wireless Emergency Call System and premature depletion of the battery.
Identifiers
| code_info | All units of the Affected Device Models sold between July 26, 2022 and June 5, 2024 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2417-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.